rs2159100
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| (C;T) | ||
| (T;T) | 2.36 increased odds of bipolar disorder |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 2237227 |
| Gene | CACNA1C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2159100 |
| dbSNP (classic) | rs2159100 |
| ClinGen | rs2159100 |
| ebi | rs2159100 |
| HLI | rs2159100 |
| Exac | rs2159100 |
| Gnomad | rs2159100 |
| Varsome | rs2159100 |
| LitVar | rs2159100 |
| Map | rs2159100 |
| PheGenI | rs2159100 |
| Biobank | rs2159100 |
| 1000 genomes | rs2159100 |
| hgdp | rs2159100 |
| ensembl | rs2159100 |
| geneview | rs2159100 |
| scholar | rs2159100 |
| rs2159100 | |
| pharmgkb | rs2159100 |
| gwascentral | rs2159100 |
| openSNP | rs2159100 |
| 23andMe | rs2159100 |
| SNPshot | rs2159100 |
| SNPdbe | rs2159100 |
| MSV3d | rs2159100 |
| GWAS Ctlg | rs2159100 |
| GMAF | 0.3053 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
23andMe blog ([PMID 18711365
]) rs1006737 or (rs2159100) Each T at this SNP increased the odds of bipolar disorder by 1.18 times compared to having two CC copies
[PMID 25453756] A role for noncoding variation in schizophrenia. This study finds evidence for rs2159100 allele T as a factor in schizophrenia.
